Package 59651-867-01

Brand: ciprofloxacin

Generic: ciprofloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59651-867-01
Digits Only 5965186701
Product NDC 59651-867
Product ID 59651-867_99cc20d5-219c-4118-83ad-77df85348735
Description

100 TABLET, FILM COATED in 1 BOTTLE (59651-867-01)

Marketing

Marketing Status
Discontinued 2028-02-29
Brand ciprofloxacin
Generic ciprofloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Ciprofloxacin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "99cc20d5-219c-4118-83ad-77df85348735", "openfda": {"upc": ["0359651866306", "0359651867303"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "197512", "309309"], "spl_set_id": ["7041828f-d4ec-4813-bcac-cb335c6c312a"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-867-01)", "package_ndc": "59651-867-01", "marketing_end_date": "20280229", "marketing_start_date": "20240209"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (59651-867-05)", "package_ndc": "59651-867-05", "marketing_end_date": "20280229", "marketing_start_date": "20240209"}], "brand_name": "Ciprofloxacin", "product_id": "59651-867_99cc20d5-219c-4118-83ad-77df85348735", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "59651-867", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_end_date": "20280229", "marketing_start_date": "20240209"}